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Creating manual annotations in a large number of images is a tedious bottleneck that limits deep learning use inmany applications. Here, we present a study in which we used the output of a classical image analysis pipeline aslabels when training a convolutional neural network (CNN). This may not only reduce the time experts spendannotating images but it may also lead to an improvement of results when compared to the output from the classicalpipeline used in training. In our application, i.e., cell nuclei segmentation, we generated the annotations usingCellProfiler (a tool for developing classical image analysis pipelines for biomedical applications) and trained onthem a U-Net-based CNN model. The best model achieved a 0.96 dice-coefficient of the segmented Nuclei and a0.84 object-wise Jaccard index which was better than the classical method used for generating the annotations by0.02 and 0.34, respectively. Our experimental results show that in this application, not only such training is feasiblebut also that the deep learning segmentations are a clear improvement compared to the output from the classicalpipeline used for generating the annotations.

Cell migration is pivotal for their development, physiology and disease treatment. A single cell on a 2D surface can utilize continuous or discontinuous migration modes. To comprehend the cell migration, an adequate quantification for single cell-based analysis is crucial. An automatized approach could alleviate tedious manual analysis, facilitating large-scale drug screening. Supervised deep learning has shown promising outcomes in computerized microscopy image analysis. However, their implication is limited due to the scarcity of carefully annotated data and uncertain deterministic outputs. We compare three deep learning models to study the problem of learning discriminative morphological representations using weakly annotated data for predicting the cell migration modes. We also estimate Bayesian uncertainty to describe the confidence of the probabilistic predictions. Amongst three compared models, DenseNet yielded the best results with a sensitivity of 87.91%±13.22 at a false negative rate of 1.26%±4.18.

The choice of an optimal feature detector-descriptor combination for image matching often depends on the application and the image type. In this paper, we propose the Log-Polar Magnitude feature descriptor—a rotation, scale, and illumination invariant descriptor that achieves comparable performance to SIFT on a large variety of image registration problems but with much shorter feature vectors. The descriptor is based on the Log-Polar Transform followed by a Fourier Transform and selection of the magnitude spectrum components. Selecting different frequency components allows optimizing for image patterns specific for a particular application. In addition, by relying only on coordinates of the found features and (optionally) feature sizes our descriptor is completely detector independent. We propose 48- or 56-long feature vectors that potentially can be shortened even further depending on the application. Shorter feature vectors result in better memory usage and faster matching. This combined with the fact that the descriptor does not require a time-consuming feature orientation estimation (the rotation invariance is achieved solely by using the magnitude spectrum of the Log-Polar Transform) makes it particularly attractive to applications with limited hardware capacity. Evaluation is performed on the standard Oxford dataset and two different microscopy datasets; one with fluorescence and one with transmission electron microscopy images. Our method performs better than SURF and comparable to SIFT on the Oxford dataset, and better than SIFT on both microscopy datasets indicating that it is particularly useful in applications with microscopy images.

The NUDIX enzymes are involved in cellular metabolism and homeostasis, as well as mRNA processing. Although highly conserved throughout all organisms, their biological roles and biochemical redundancies remain largely unclear. To address this, we globally resolve their individual properties and inter-relationships. We purify 18 of the human NUDIX proteins and screen 52 substrates, providing a substrate redundancy map. Using crystal structures, we generate sequence alignment analyses revealing four major structural classes. To a certain extent, their substrate preference redundancies correlate with structural classes, thus linking structure and activity relationships. To elucidate interdependence among the NUDIX hydrolases, we pairwise deplete them generating an epistatic interaction map, evaluate cell cycle perturbations upon knockdown in normal and cancer cells, and analyse their protein and mRNA expression in normal and cancer tissues. Using a novel FUSION algorithm, we integrate all data creating a comprehensive NUDIX enzyme profile map, which will prove fundamental to understanding their biological functionality.

Image-based screening typically produces quantitative measurements of cell appearance. Large-scale screens involving tens of thousands of images, each containing hundreds of cells described by hundreds of measurements, result in overwhelming amounts of data. Reducing per-cell measurements to the averages across the image(s) for each treatment leads to loss of potentially valuable information on population variability. We present PopulationProfiler-a new software tool that reduces per-cell measurements to population statistics. The software imports measurements from a simple text file, visualizes population distributions in a compact and comprehensive way, and can create gates for subpopulation classes based on control samples. We validate the tool by showing how PopulationProfiler can be used to analyze the effect of drugs that disturb the cell cycle, and compare the results to those obtained with flow cytometry.